FDA Recall United States Terminated Historical recordClass II
Jindilli Beverages LLC
- Product
- Milkadamia Salted Buttery Spread 8 ounces packaged in plasti…
- Reason
- Potential to contain mold
- Published
- June 3, 2020
- Distribution
- Nationwide
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Recall totals
All FDA and USDA recalls in Public Health Trace, June 2012 to September 2026.
37,118
Total recall recordsAll FDA and USDA recalls in Public Health Trace9,793
Class I recallsReasonable probability of serious health consequences24,343
Class II recallsTemporary or medically reversible health consequences2,887
Class III recallsNot likely to cause adverse health consequencesQuick insights
A snapshot of the most notable patterns across all recorded FDA and USDA recalls.
Most recalled product100 vegetarian Fenugreek Capsules 90 count, 600mg, packaged in 150cc Amber Glass Packer with White Polypropylene Cap.
53 recalls
Most common hazardLack of Assurance of Sterility
2,072 recalls
Newest recallhttp://www.fda.gov/safety/recalls-market-withdrawals-safety-alerts/gf-blends-recalls-truly-aip-all-purpose-flour-and-bread-mix-and-eat-gangster-flat-bread-pizza-mixPublished September 18, 2026
Download matching recalls as CSV
CSV exports include up to 5,000 matching rows (applying your current filters), not the full dataset if it's larger.
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A chart of recalls grouped by month.
Download CSVSummary (Year to date)
- 1,527 recalls have been announced year to date.
- Aug 2026 was 24% lower than the previous complete period (Jul 2026: 240).
- The highest complete period was Jun 2026 (297).
- Sep 2026 is incomplete and not included in the figures above.
- Complete data
- Incomplete
A bar chart of the total number of recalls in this dataset by recall class.
| Class | Recalls |
|---|---|
| Class II | 24,343 |
| Class I | 9,793 |
| Class III | 2,887 |
| Not Yet Classified | 1 |
| Class | Recalls |
|---|---|
| Class II | 24,343 |
| Class I | 9,793 |
| Class III | 2,887 |
| Not Yet Classified | 1 |
FDA Recall United States Terminated Historical recordClass II
Jindilli Beverages LLC
- Product
- Milkadamia Unsalted Buttery Spread 8 ounces packaged in plas…
- Reason
- Potential to contain mold
- Published
- June 3, 2020
- Distribution
- Nationwide
FDA Recall United States Ongoing Historical recordClass II
Absorb Health LLC
- Product
- Absorb Health Advanced Joint Relief Joint Health; 510mg; 90…
- Reason
- The firm was notified by the FDA that they failed to included a shellfish allergen on their ingredient panel.
- Published
- June 3, 2020
- Distribution
- Product was shipped to the following sta…
FDA Recall United States Terminated Historical recordClass II
GARZA FOOD VENTURES
- Product
- Siete Grain Free Cashew Flour Tortillas NET WT 7 OZ (200g) 8…
- Reason
- Potential to contain foreign material.
- Published
- June 3, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Ethacrynic Acid Tablets USP, 25 mg, 100 Tablets per Bottle, Rx only, Distr. by: West-Ward Pharmaceuticals Corp., Eatontown, NJ 07724, NDC: 0054-0415-25.
- Reason
- Failed Impurities/Degradation Specifications: Out of Specification for impurity 6 and total degradants.
- Published
- May 27, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Gabapentin Tablets USP, 600 mg, Rx Only, 500-count bottle, Manufactured for: Exelan Pharmaceuticals, Inc., Lawrenceville, GA 30046, Manufactured by: InvaGen Pharmaceuticals, Inc., Hauppauge, NY 11788, NDC 76282-405-05.
- Reason
- Failed Impurities/Degradation Specifications; failure of Impurity A test at the 12-month long-term stability testing.
- Published
- May 27, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass II
Aloprim (allopurinol sodium) for Injection, 500 mg Single-Dose Vial, Rx only, Manufactured for: Mylan Institutional LLC, Rockford, IL 61103 USA. NDC: 67457-187-50
- Reason
- Discoloration: Out-of-specification results for appearance obtained during routine stability testing at the end of shelf-life for the parameters Appearance and Color of Solution.
- Published
- May 27, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass I
LACTATED RINGER'S Injection, USP 1000 mL flexible container, Rx Only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7953-09
- Reason
- Presence of Particulate Matter: confirmed customer complaint for the presence of particulate matter identified as iron oxide.
- Published
- May 27, 2020
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass I
Ramar International Corporation
- Product
- Peekaboo Ice Cream + hidden Veggies; Organic Mint Chocolate…
- Reason
- Ice cream that tested positive for Listeria monocytogenes was to be held and destroyed but was found on retail shelves.
- Published
- May 27, 2020
- Distribution
- FL
FDA Recall Terminated Historical recordClass I
Finasteride Plus 1.25 mg Capsule, a) 30-count bottle, b) 90-count bottle, Compounded Product Not for Resale, MasterPharm, 115-02 Liberty Ave, Richmond Hill, NY 11419.
- Reason
- Cross Contamination with Other Products; Finasteride Plus 1.25mg capsules were found to contain minoxidil.
- Published
- May 20, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
ChapStick Total Hydration Moisture + Tint + SPF15 Pretty in Pink Net Wt. 0.08 OZ (2.2g) Marketed by: Pfizer, Madison, NJ 07940 USA NDC 0573-0873-08
- Reason
- Labeling: Not elsewhere classified: Observed separation in the secondary packaging in the blister and the backer card
- Published
- May 20, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
ChapStick Total Hydration Moisture + Tint + SPF15 Very Berry Net Wt. 0.08 OZ (2.2g) Marketed by: Pfizer, Madison, NJ 07940 USA NDC 0573-0872-08
- Reason
- Labeling: Not elsewhere classified: Observed separation in the secondary packaging in the blister and the backer card
- Published
- May 20, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
ChapStick Total Hydration Moisture + Tint + SPF15 Peachy Keen Net Wt. 0.08 OZ (2.2g) Marketed by: Pfizer, Madison, NJ 07940 USA, NDC 0573-0871-08
- Reason
- Labeling: Not elsewhere classified: Observed separation in the secondary packaging in the blister and the backer card
- Published
- May 20, 2020
- Distribution
- Nationwide
FDA Recall Terminated Historical recordClass III
Memantine Hydrochloride Extended-Release Capsules, 28 mg, 100 capsules per unit dose cartons, Rx only, Manufactured by: Lupin Limited, Pithampur (M.P.)-454 775, India; Distributed by: Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 47152 USA. NDC: 0904-6735-61
- Reason
- Failed dissolution specifications: Low stage 3 results obtained for dissolution during routine stability testing.
- Published
- May 20, 2020
- Distribution
- Multiple states
FDA Recall United States Terminated Historical recordClass II
Natural Dairy Products
- Product
- Common Market 1 % Milk (1/2 Gallon)
- Reason
- A sample of the product was found to be positive with Antibiotic Residue.
- Published
- May 20, 2020
- Distribution
- The product was distributed to the follo…
FDA Recall United States Terminated Historical recordClass II
Natural Dairy Products
- Product
- Fairway Market 1 % Milk (1/2 gallon and gallon)
- Reason
- A sample of the product was found to be positive with Antibiotic Residue.
- Published
- May 20, 2020
- Distribution
- The product was distributed to the follo…
FDA Recall United States Terminated Historical recordClass II
Natural Dairy Products
- Product
- Natural by Nature 1 % Milk (gallon, 1/2 gallon, and quart)
- Reason
- A sample of the product was found to be positive with Antibiotic Residue.
- Published
- May 20, 2020
- Distribution
- The product was distributed to the follo…
FDA Recall Terminated Historical recordClass II
Infuvite PEDiatric Pharmacy, kit in 1 carton (40 mL fill in a 50 mL) vial 1 and (10 mL) in vial 2, Rx Only, Distributed by: Baxter Healthcare Corporation Clintec Nutrition Division Deerfield, IL 60015 USA, NDC 54643-5647-0
- Reason
- Defective Container: Sub-optimal crimping in vial of Pediatric Infuvite Multiple Vitamins
- Published
- May 13, 2020
- Distribution
- Nationwide
FDA Recall United States Terminated Historical recordClass II
Glaxosmithkline Consumer Healthcare Holdings
- Product
- Benefiber Prebiotic Fiber Supplement, packaged in the follow…
- Reason
- Fiber prebiotic product potentially contaminated with small plastic pieces
- Published
- May 13, 2020
- Distribution
- Distributed to the following US states:…
FDA Recall United States Terminated Historical recordClass II
Glaxosmithkline Consumer Healthcare Holdings
- Product
- Benefiber Healthy Shape Prebiotic Fiber Supplement, 500G UP…
- Reason
- Fiber prebiotic product potentially contaminated with small plastic pieces
- Published
- May 13, 2020
- Distribution
- Distributed to the following US states:…
Data last updated:
Recall records are summarized from official FDA and USDA sources. Notices may be updated, reclassified, terminated, or withdrawn. Always review the linked official notice for the most current instructions. Read the full medical disclaimer.
